rs397508834

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(-;C)	6	BRCA1 variant considered pathogenic for breast cancer
(C;C)	0	common in clinvar

Make rs397508834(-;-)

Reference

GRCh38 38.1/141

Chromosome

17

Position

43094440

Gene

BRCA1

is a	snp
is	mentioned by
dbSNP	rs397508834
ClinGen	rs397508834
ebi	rs397508834
HLI	rs397508834
Exac	rs397508834
Varsome	rs397508834
Map	rs397508834
PheGenI	rs397508834
hapmap	rs397508834
1000 genomes	rs397508834
hgdp	rs397508834
ensembl	rs397508834
gopubmed	rs397508834
geneview	rs397508834
scholar	rs397508834
google	rs397508834
pharmgkb	rs397508834
gwascentral	rs397508834
openSNP	rs397508834
23andMe	rs397508834
23andMe all	rs397508834
SNP Nexus
SNPshot	rs397508834
SNPdbe	rs397508834
MSV3d	rs397508834
GWAS Ctlg	rs397508834

Max Magnitude

6

ClinVar
Risk	rs397508834(-;-)
Alt	rs397508834(-;-)
Reference	Rs397508834(C;C)
Significance	Pathogenic
Disease	Familial cancer of breast Breast-ovarian cancer
Variation	info
Gene	BRCA1
CLNDBN	Familial cancer of breast Breast-ovarian cancer, familial 1
Reversed	1
HGVS	NC_000017.10:g.41246457delG
CLNSRC	ClinVar
CLNACC	RCV000047337.2, RCV000257589.2,